Woojeon Company
Country not established FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
FDA establishments
- Woojeon Co. Gunpo-si Gyeonggi · KR FEI 3010201636
Frequently asked questions
How many devices does Woojeon Company have in the registry?
The registry currently lists 1 device for Woojeon Company. Devices recorded under merged duplicate company entries are counted once.
Which registries list Woojeon Company's devices?
Among its 1 most recently registered device, Woojeon Company has devices listed in FDA 510(k) (1 device).
What risk classes do Woojeon Company's devices fall under?
Among its 1 most recently registered device, the classes recorded for Woojeon Company's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Woojeon Company in the registry?
The most recently registered devices listed for Woojeon Company include WOOJEON ACUPUNCTURE NEEDLE (=SERA ACUPUNCTURE NEEDLE).
Which FDA establishments are linked to Woojeon Company?
1 FDA establishment is linked to Woojeon Company in the registry; they are listed on the company page.